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Reaction of N-(1-cyano-1-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- And 2-thienyl magnesium bromides: A new approach to alkylaromatic α-hydroxyaminoketones Full article

Journal Mendeleev Communications
ISSN: 0959-9436
Output data Year: 1996, Volume: 6, Number: 5, Pages: 202-203 Pages count : 2 DOI: 10.1070/MC1996v006n05ABEH000646
Authors Khlestkin V.K. 1 , Reznikov V.A. 1 , Mazhukin D.G. 1 , Tikhonov A.Ya. 1 , Volodarsky L.B. 1
Affiliations
1 Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

Abstract: The reaction of N-(1-cyano-1-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides affords 3-imidazolines which hydrolyse to alkylaromatic α-hydroxyaminoketones, synthons for stable nitroxides.
Cite: Khlestkin V.K. , Reznikov V.A. , Mazhukin D.G. , Tikhonov A.Y. , Volodarsky L.B.
Reaction of N-(1-cyano-1-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- And 2-thienyl magnesium bromides: A new approach to alkylaromatic α-hydroxyaminoketones
Mendeleev Communications. 1996. V.6. N5. P.202-203. DOI: 10.1070/MC1996v006n05ABEH000646 Scopus РИНЦ OpenAlex
Dates:
Published print: Jan 1, 1996
Identifiers:
Scopus: 2-s2.0-25044480548
Elibrary: 13249517
OpenAlex: W2951455027
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